Analyte Meter Protectors and Methods

ABSTRACT

Analyte meter protectors, meters that include the same, and methods.

This application claims priority to U.S. Provisional Application Ser. No. 60/871,910 that was filed with the United States Patent and Trademark Office on Dec. 26, 2006. The entire disclosure of U.S. Provisional Application Ser. No. 60/871,910 is incorporated by reference.

BACKGROUND OF THE INVENTION

Analytical testers, also sometimes referred to as sensors, are commonly used to monitor the level of an analyte in a body fluid. For example, diabetics use analyte testers to monitor body glucose levels.

Analyte testing may involve testing once per day, but typically should be carried out periodically throughout the day using multiple analyte testers-one tester for each test. To “read” a tester, i.e., to analyze the body fluid applied to a tester and determine one or more analyte levels, a tester reader, oftentimes referred to as a “meter”, is used. Either before or after a sample of body fluid is applied to a tester, the tester is received by the meter. The meter performs various functions and analyzes the tester-applied sample to provide an analyte level to the user.

The tester receiving area of a meter, commonly referred to as a tester “port”, is the opening in a meter that receives a tester for testing. The tester port is therefore an opening from the outside meter environment to the interior of the meter. Because the interior is exposed to the outside environment via the tester port, the potential for contaminating materials to enter the meter's interior through the port exists. For example, unintended fluid ingress into the port from blood, interstitial fluid, control solution, cleaning fluid, or other fluids may occur. This unintended fluid ingress may interfere with the readings and confound the analyte results. Given the importance of obtaining accurate analyte level readings, it is imperative that the meter does not become contaminated.

Accordingly, as meters continue to be used for analyte monitoring, there continues to be an interest in analyte monitoring devices that are protected from contamination. Of interest are port protectors that are easily removable and replaceable, e.g., disposable.

SUMMARY OF THE INVENTION

Analyte testing medical devices, and components for use with the same, as well as methods of using the medical devices and components for analyte testing are provided.

Various embodiments include a meter port protector attachable to an area of a meter tester port. In many embodiments, a protector is disposable, e.g., easily removable and attachable.

In certain embodiments, a protector includes a slot for receiving an analyte tester. The slot may be dimensioned to provide minimal clearance between a surface of the slot and a surface of a received tester. For example, in certain embodiments a protector slot may be dimensioned to swipe or squeegee across a fluid-containing surface of a received tester. This may be useful to prevent unwanted fluid from entering the tester port of the meter and/or to meter the sample.

In many embodiments, the area defined by the opening of a protector is less than the area defined by the port of a meter. In this manner, the size of the opening to the meter is reduced by the protector.

Embodiments also include self aligning protectors. These protectors include features that correctly position the protectors with corresponding meters.

Also provided are analyte meters that include a tester port. Embodiments include meters having port protector removably secured about the ports. In certain embodiments, the protectors include a slot for receiving a tester.

Also included are methods, where embodiments include attaching, e.g., permanently or temporarily, a port protector about a port area of a meter. In certain embodiments, the methods include attaching a protector to a meter to reduce the size of the area defined by the meter port. Embodiments also include removing a first port protector from a meter and attaching a second protector to the meter. This may be particularly useful in hospital or analogous settings in which a single meter may be used to read a plurality of testers, at least some of which may be testing sample from different individuals.

Various methods may be employed to connect a protector to meter. Such methods include removable connecting a protector to a meter, e.g., using an adhesive, releasable tabs, etc.

Also provided are systems and kits that include an analyte meter and/or port protector and/or analyte tester, and/or lancing device. In certain embodiments, a plurality of protectors may be provided to a user, e.g., bundled together such as in a kit.

These and various other features which characterize the invention are pointed out with particularity in the attached claims. For a better understanding of the testers of the invention, their advantages, their use and objectives obtained by their use, reference may be made to the drawings and to the accompanying description, in which there is illustrated and described various embodiments of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

Referring now to the drawings, wherein like reference numerals and letters indicate corresponding structure throughout the several views:

FIG. 1 is an isometric front view of an exemplary embodiment of an analyte meter;

FIG. 2A is an isometric front view of an exemplary embodiment of a port protector; FIGS. 2B and 2C are isometric rear views of the protector of FIG. 2A; and

FIG. 3 is an isometric front view of the meter of FIG. 1 with the protector of FIGS. 2A-2C installed thereon.

DETAILED DESCRIPTION

As summarized above, protectors positionable about a tester opening or port of an analyte monitoring device are provided. The protectors are designed to mate with meters and more specifically mate with port areas. The protectors are particularly useful in preventing contaminants from entering the meters through the tester ports.

The protectors may be adapted to be used with any medical device having an opening and are particularly useful as adapted to be used with an analyte monitoring medical device having an opening for receiving a tester (also referred to as a test strip or sensor), such as an in vitro analyte monitoring meter or in vivo analyte monitoring system, e.g., those provided by Abbott Diabetes Care Inc. of Alameda, Calif.

Port-containing meters may be electrochemical or optical meters, and may be configured to determine the level of one or more analytes, where analytes include, but are not limited to, glucose, blood β-ketone, ketone bodies, lactate, acetyl choline, amylase, bilirubin, cholesterol, chorionic gonadotropin, creatine kinase (e.g., CK-MB), creatine, DNA, fructosamine, glucose, glutamine, growth hormones, hormones, ketones, lactate, peroxide, prostate-specific antigen, prothrombin, RNA, thyroid stimulating hormone, and troponin, in sample of body fluid. Meters may also be configured to determined the concentration of drugs, such as, for example, antibiotics (e.g., gentamicin, vancomycin, and the like), digitoxin, digoxin, drugs of abuse, theophylline, and warfarin, may also be determined and the like, in a sample of body fluid. In certain embodiments, the protectors are shaped and sized to cooperate with a FreeStyle® brand blood glucose monitoring meter or a Precision® brand blood monitoring meter capable of monitoring glucose and ketones, or other such analyte meters. The protectors may find use in meters designed for use in a hospital or similar clinic environment where a single meter may be used for a plurality of patients. Such systems include, but are not limited to, Precision PCx meters and FreeStyle Connect meters and Precision Xceed Pro manufactured by Abbott Diabetes Care.

In certain embodiments, the protectors may be configured to mate with a port of a continuous analyte monitoring system. For example, a continuous glucose monitoring system may include a component that receives analyte data from a transcutaneously positioned or wholly implanted inserted glucose sensor, and which component may be configured to communicate analyte results to the user, e.g., audibly by way of a display, or visually. The continuous monitoring system receiver may include a conventional blood glucose meter and therefore a port for accepting a glucose tester. For example, an analyte meter may be incorporated into a module of a continuous analyte monitoring system, e.g., a transmitter module, receiver module, etc. Such may be convenient for calibrating and/or confirming the continuous system. The conventional meter and test strip may be used to calibrate the continuous system (see for example U.S. Pat. No. 6,175,752), e.g., using one point calibration or other calibration protocol. It is to be understood that meters includes stand alone meters, as well those operably connected to, e.g., integrated with) continuous analyte monitoring systems. Exemplary testers and meters and continuous analyte monitoring systems (sometimes referred to as in vivo system) include testers and meters such as those described, e.g., in U.S. Pat. No. 6,071,391; 6,120,676; 6,143,164; 6,299,757; 6,338,790; 6,377,894; 6,600,997; 6,773,671; 6,514,460; 6,592,745; 5,628,890; 5,820,551; 6,736,957; 4,545,382; 4,711,245; 5,509,410; 6,540,891; 6,730,200; 6,764,581; 6,299,757; 6,338,790; 6,461,496; 6,503,381; 6,591,125; 6,616,819; 6,618,934; 6,676,816; 6,749,740; 6,893,545; 6,942,518; 6,175,752; and 6,514,718, and elsewhere. In certain embodiments, the port may be included in, e.g., integrated, a drug delivery system, e.g., in an insulin pump module such a pump or controller module thereof.

In certain embodiments, ports may include a tester slot. A slot is a passage through the body of the protector. Such a slot is dimensioned to admit an analyte tester. As such, certain embodiments include slots that are alignable with a meter port when the protector is connected to the meter. In this manner, when a protector is positioned about a meter port, a tester may be easily passed through the protector slot and into the port.

The slots may be any suitable dimension. In certain embodiments, a slot may be sized and shaped to provide minimal clearance between at least one surface of the slot and at lest one surface of a received tester. For example, clearance may be one the order of millimeters, e.g., less than about 2.5 mm, e.g., less than about 1 mm. In certain embodiments at least one surface of a protector slot may be configured to contact at least one surface of tester, e.g., to swipe or squeegee across a fluid-containing surface of a received tester. This may be useful to prevent unwanted fluid from entering the tester port of the meter and/or to meter the sample.

In many embodiments, the area defined by the opening of a protector is less than the area defined by the port of a meter. In this manner, the size of the opening to the meter is reduced by the protector. For example, in certain embodiments, the area defined by a slot of a protector may be less than 100% of the area defined by a port of a meter to which it is attachable, e.g., the area defined by a slot of a protector may be less than 100% of the area defined by a port of a meter, e.g., may be less than 80% of area defined by a port of a meter.

The slots may be any suitable shape. The shape may depend at least in part on the shape of the tester the meter is designed to accept. In certain embodiments, the slots may be substantially rectangular, e.g., in instances in which a substantially rectangular tester is employed. Other slot shapes may of course be used as well.

In certain embodiments, the slot may include a flexible valve that is disposed at least partially across the slot, and in some embodiments completely across the slot. The flexible valve may include self-sealing slit(s) which open to permit a tester therethrough in response to increased pressure on the slits, e.g., by a tester being pushed there against.

In many embodiments, the protectors do not apply pressure to a tester received in the slot of the protector.

Port protectors may be fixedly attached/attachable to a meter, or may be wholly removable from a meter. For example, a protector may be attachable to a meter over the port, but yet easily removable by a user when access to the tester port is desired and/or when replacement with another protector is desired. One or more engagement features may be used. An engagement feature(s) may be positioned on a protector and/or a meter. In certain embodiments adhesive is employed on a meter-contacting surface of a protector. The adhesive may be any suitable adhesive, such as contact adhesives, pressure sensitive adhesives, glues, epoxies, adhesive resins, and the like. In certain embodiments, the adhesive is applied to a membrane of suitable thickness, e.g. foam. The adhesive may be covered by a removable release liner to protect the adhesive from the environment until use. The release liner may be any convenient material, where representative release films include polyesters, such as PET or PP, and the like.

In certain embodiments molded features may be used. Such features may help to attach a protector to a meter and/or align a protector with the meter, e.g., particularly for embodiments that include a slot. Molded features may be used to align the protector slot with the port so that a tester may pass through the slot and into the port. For example, a rib(s) or tab(s) may be used. One or more ribs (on a protector and/or meter) may cooperate with a mating feature. Embodiments also include protectors configured to snap fit and/or friction fit with a meter. In certain embodiments, a meter-contacting surface of a protector may have a form that corresponds to a meter's surface, e.g., may be a negative of a meter surface. In certain embodiments, a portion of a protector may be fixedly attached to a meter, allowing the unattached portion to move away from the meter. This may be useful for cleaning the protector. In certain embodiments, the interface of a coupled meter and protector provides a a substantially fluid tight seal.

In certain embodiments, a protector may also be configured to guide a tester into a port. For example, a protector having a slot may include guides, rails, channels, indentions, recessed structures, elevated structures, clamps, or the like, about the slot. Certain embodiments include a ledge. The ledge may be an extension of a slot, e.g., a bottom of a slot may include ledge. It will be appreciated that words such as “top”, “bottom”, “upper”, and “lower”, and the like, are used in a relative sense only. In certain embodiments, a protector may include spaced apart guides. With this or analogous configurations, a tester may be slid into position along the guides. The guides may be dimensioned such that a tester is snugly fit between the guides when it is mounted between the guides. During positioning of the tester, portions of the tester may be gripped (such as with a user's fingers) and the gripped portions used to then slide the tester into the mounted position between the guides.

The protectors may be made of any suitable material and may be substantially rigid or substantially flexible. In certain embodiments, the material is substantially flexible. Elastomeric materials may be used, e.g., rubber, or other compliant material. For example, foam may be used. In certain embodiments, the material may be a thermoplastic elastomer (TPE), thermoplastic urethane (TPU), polycarbonate (PC), acrylonitrile butadiene-styrene (ABS) or a combination of two or three of these. In certain embodiments, a protector has a hard plastic frame (e.g., PC-ABS) with a compliant area around the port opening.

Referring now to the Figures, FIG. 1 shows an isometric front view of an exemplary embodiment of an analyte meter 10. Meter 10 includes housing 12 defining an interior space and having a tester port 14 for receiving a tester. An exemplary analyte tester 20 is shown positioned in port 14 to be read by the meter. Analyte tester 20, e.g., a glucose tester, is shown as having a generally rectangular shape, but it is understood that any shaped tester may be used. Analyte tester 20 can be any tester suitable for use with meter 10. Examples of testers 20 are disclosed, for example, in U.S. Pat. Nos. 6,299,757, 6,591,125, and 6,616,819. The tester may have a sample chamber volume, for receive of sample (e.g., blood) to be tested, of no more than about 1 microliter, and in some embodiments, a volume of no more than about 0.5 microliter or even no more than 0.2 microliter.

This particular meter embodiment of FIG. 1 includes engagement detents 16. Detents 16 are configured to retain a port protector.

FIG. 2A shows an isometric front view of an exemplary embodiment of a port protector 30. Protector 30 includes a body 31. Within body 31 is formed slot 32. While the embodiment of FIG. 2A includes a slot, as noted above, certain embodiments do not include slots. In those embodiments that do not include a slot, the protector may be formed as a plug that cooperates with the port.

Protector 30 also includes tester positioning feature(s), in this embodiment in the form of guide grooves 33 positioned on opposing sides of the protector and a ledge or “diving board” feature 34.

Protector 30 also includes attachment features. FIGS. 2B and 2C show isometric rear views of protector 30 showing engagement ribs 35. Attachment features 35 in this embodiment are in the form of engagement protrusions that extend outwardly from the protector. In certain embodiments the form of engagement may be indentations extending inwardly into the protector. Attachment features also serve to align the protector with the meter.

Engagement ribs 35 mate with detents on a meter, to hold the protector in place on the meter. Some or all of the back surface of protector 35 shown in FIGS. 2B and 2C may include adhesive thereon. Adhesive may be in addition to or in place of engagement ribs 35.

FIG. 3 shows an isometric front view of meter 10 with protector 30 installed thereon. As shown, the protector narrows the opening to the interior of the meter.

To perform an analyte test, a sample of biological fluid is provided to the tester for analyte testing, where the level of analyte is determined. Sample may be applied to the tester before or after the tester is positioned in the meter. In many embodiments, it is the level of glucose in blood, interstitial fluid, and the like, that is determined. Also in many embodiments, the source of the biological fluid is a drop of blood drawn from a patient, e.g., after piercing the patient's skin with a lancing device or the like.

The invention has been described with reference to various specific and preferred embodiments and techniques. However, it will be apparent to one of ordinarily skill in the art that many variations and modifications may be made while remaining within the spirit and scope of the invention.

All patents and other references in this specification are indicative of the level of ordinary skill in the art to which this invention pertains. All patents and patent applications are herein incorporated by reference to the same extent as if each individual patent was specifically and individually incorporated by reference. 

1.-29. (canceled)
 30. An analyte monitoring device, comprising: an electrochemical sensor configured to produce one or more signals indicative of an analyte concentration of a sample; a housing comprising a port for receiving the electrochemical sensor; a port protector comprising an opening and attached to the housing about the port to prevent contaminants from entering the interior of the housing while allowing the electrochemical sensor to be received through the opening of the port protector; a processor housed in the housing, wherein the processor is configured to process one or more signals produced by the electrochemical sensor and thereby determine the analyte concentration, and wherein the processor is configured to determine a dosage of medication based at least in part on the determined analyte concentration; and a display in communication with the processor, wherein the display is configured to display the determined dosage of medication.
 31. The analyte monitoring device of claim 30, wherein the port protector provides a substantially fluid tight seal with the housing.
 32. The analyte monitoring device of claim 30, wherein the port protector is removably attachable to the analyte monitoring device.
 33. The analyte monitoring device of claim 30, wherein the port protector is fixedly attachable to the analyte monitoring device.
 34. The analyte monitoring device of claim 30, wherein the port protector comprises an elastomeric material.
 35. The analyte monitoring device of claim 34, wherein the port protector comprises rubber.
 36. The analyte monitoring device of claim 34, wherein the port protector comprises adhesive.
 37. The analyte monitoring device of claim 30, wherein the opening of the port protector comprises a guide for receiving the electrochemical sensor.
 38. The analyte monitoring device of claim 37, wherein the guide comprises a ledge.
 39. The analyte monitoring device of claim 30, wherein the analyte is glucose.
 40. The analyte monitoring device of claim 39, wherein the medication is insulin.
 41. The analyte monitoring device of claim 30, wherein the port protector reduces the size of the port when attached to the housing.
 42. The analyte monitoring device of claim 30, wherein the display is a liquid crystal display (LCD).
 43. The analyte monitoring device of claim 30, wherein the display is a light-emitting diode (LED) display.
 44. The analyte monitoring device of claim 30, wherein the display comprises a backlight.
 45. The analyte monitoring device of claim 44, wherein the backlight is activated upon insertion of the electrochemical sensor into the port.
 46. The analyte monitoring device of claim 39, wherein the display comprises one or more indicators activatable when the analyte concentration indicates a state of hyperglycemia, hypoglycemia, impending hyperglycemia or impending hypoglycemia.
 47. The analyte monitoring device of claim 46, wherein the one or more indicators are color-coded.
 48. The analyte monitoring device of claim 30, wherein the display is configured to display a graph of the analyte concentration over a period of time.
 49. The analyte monitoring device of claim 30, wherein the display is configured to display a graph of rate of change or acceleration in the rate of change of the analyte concentration over time.
 50. The analyte monitoring device of claim 30, wherein the display is configured to display a message in the form of text directing a user of the analyte monitoring device to perform an action in response to the determined analyte concentration.
 51. The analyte monitoring device of claim 30, further comprising a transmitter in communication with the processor, wherein the transmitter is configured to transmit data related to the determined analyte concentration.
 52. The analyte monitoring device of claim 51, wherein the transmitter is configured to transmit the data wirelessly.
 53. The analyte monitoring device of claim 52, wherein the transmitter is configured to transmit the data using a radio frequency (RF) transmission.
 54. The analyte monitoring device of claim 52, wherein the computer is located in a doctor's office.
 55. The analyte monitoring device of claim 30, wherein the processor is configured to determine if the analyte concentration, rate of change, and/or acceleration in the rate of change of the analyte concentration exceeds or meets one or more threshold values.
 56. The analyte monitoring device of claim 55, wherein the processor is configured to activate an alarm in the event the one or more threshold values are met or exceeded.
 57. The analyte monitoring device of claim 30, wherein the processor is configured to evaluate trends in analyte concentration based on a series of sensor signals.
 58. The analyte monitoring device of claim 57, wherein the processor is further configured to predict trends in the analyte concentration.
 59. The analyte monitoring device of claim 58, wherein the trends comprise rate and/or acceleration of analyte concentration increase or decrease.
 60. A glucose monitoring device, comprising: an electrochemical sensor configured to produce one or more signals indicative of glucose concentration of a sample; a housing comprising a port for receiving the electrochemical sensor; a port protector comprising an opening and attached to the housing about the port to prevent contaminants from entering the interior of the housing while allowing the electrochemical sensor to be received through the opening of the port protector; a processor housed in the housing, wherein the processor is configured to process one or more signals produced by the electrochemical sensor and thereby determine the glucose concentration, and wherein the processor is configured to determine a dosage of medication based at least in part on the determined glucose concentration; and a display in communication with the processor, wherein the display is configured to display the determined dosage of medication.
 61. The glucose monitoring device of claim 60, wherein the port protector provides a substantially fluid tight seal with the housing.
 62. The glucose monitoring device of claim 60, wherein the port protector is removably attachable to the glucose monitoring device.
 63. The glucose monitoring device of claim 60, wherein the port protector is fixedly attachable to the glucose monitoring device.
 64. The glucose monitoring device of claim 60, wherein the port protector comprises an elastomeric material.
 65. The glucose monitoring device of claim 64, wherein the port protector comprises rubber.
 66. The glucose monitoring device of claim 64, wherein the port protector comprises adhesive.
 67. The glucose monitoring device of claim 60, wherein the opening of the port protector comprises a guide for receiving the electrochemical sensor.
 68. The glucose monitoring device of claim 67, wherein the guide comprises a ledge.
 69. The glucose monitoring device of claim 60, wherein the medication is insulin.
 70. The glucose monitoring device of claim 60, wherein the display comprises one or more indicators activatable when the glucose concentration indicates a state of hyperglycemia, hypoglycemia, impending hyperglycemia or impending hypoglycemia.
 71. The glucose monitoring device of claim 60, further comprising a transmitter in communication with the processor, wherein the transmitter is configured to transmit data related to the determined glucose concentration.
 72. The glucose monitoring device of claim 71, wherein the transmitter is configured to transmit the data wirelessly or using a radio frequency (RF) transmission. 